Kohn K W
Laboratory of Molecular Pharmacology, Division of Basic Sciences, National Cancer Institute, Bethesda, Maryland 20892, USA.
Mol Biol Cell. 1999 Aug;10(8):2703-34. doi: 10.1091/mbc.10.8.2703.
Eventually to understand the integrated function of the cell cycle regulatory network, we must organize the known interactions in the form of a diagram, map, and/or database. A diagram convention was designed capable of unambiguous representation of networks containing multiprotein complexes, protein modifications, and enzymes that are substrates of other enzymes. To facilitate linkage to a database, each molecular species is symbolically represented only once in each diagram. Molecular species can be located on the map by means of indexed grid coordinates. Each interaction is referenced to an annotation list where pertinent information and references can be found. Parts of the network are grouped into functional subsystems. The map shows how multiprotein complexes could assemble and function at gene promoter sites and at sites of DNA damage. It also portrays the richness of connections between the p53-Mdm2 subsystem and other parts of the network.
最终,为了理解细胞周期调控网络的整合功能,我们必须以图表、图谱和/或数据库的形式来组织已知的相互作用。我们设计了一种图表规范,能够明确表示包含多蛋白复合物、蛋白质修饰以及作为其他酶底物的酶的网络。为便于与数据库建立联系,每个分子物种在每个图表中仅用符号表示一次。分子物种可通过索引网格坐标定位在图谱上。每次相互作用都可参考一个注释列表,在其中能找到相关信息和参考文献。网络的各个部分被分组为功能子系统。该图谱展示了多蛋白复合物如何在基因启动子位点和DNA损伤位点组装并发挥作用。它还描绘了p53-Mdm2子系统与网络其他部分之间丰富的连接。